Canonical Allele Identifier: PA2827005531
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu1647Phe
CA022293
NM_001318827.2:c.4939C>T